Biodegradable disposable syringe

ABSTRACT

The present invention relates to a biodegradable disposable syringe and more particularly, to the biodegradable disposable syringe by using a novel polyester resin composition under a specific injection molding condition, thus being able to be disposed of without causing environmental contamination.

BACKGROUND OF THE INVENTION

1. Field of the Invention

The present invention relates to a biodegradable disposable syringe andmore particularly, to the biodegradable disposable syringe by using anovel polyester resin composition under a specific injection moldingcondition, thus being able to be disposed of without causingenvironmental contamination.

2. Description of the Related Art

In general, biodegradable resins have been welcomed worldwide since theycan be disposed of without causing environmental contamination and thustheir uses are on the gradual increase these days.

There have been known various kinds of biodegradable resins, however,they have not been applicable to commercial products because eithertheir applications were too limited or their physical properties andbiodegradability were not well qualified for good molding and qualityproducts.

The aliphatic polyester, known to have a good biodegradable property aof Macromol. SCI-Chem., A-23(3), 1986, pp. 393-409), have been used asmaterials in medical, agricultural, fishing and packaging industries andits fields of applications are on gradual growth. However, theconventional type of aliphatic polyesters had disadvantages that theirbackbone structures were too soft and heat-labile, it had lowcrystallinity, low melting point, difficulty in molding due to high meltindex, poor tensile strength and tear strength. To make these aliphaticpolyesters more applicable, many efforts have been exerted to increasethe number average molecular weight of the current aliphatic polyesterto have more than 30,000, however, it has not been able to obtainaliphatic polyester having a molecular weight greater than 15,000 in theconventional polycondensation system.

As a way to solve these problems conventional polyesters, a method ofmanufacturing aliphatic polyester resin having a number averagemolecular weight of greater than 30,000 by adjusting factors such asreaction temperature, degree of vacuum and amount of catalysts wasdisclosed in Korean Unexamined Patent Publication No 95-758; however,said aliphatic polyester resin had a low weight average molecular weightand was also heat-labile thus not considered appropriate in molding orforming.

In Korean Unexamined Patent Publication No 95-11.4171, a method ofmanufacturing aliphatic polyester with a high molecular weight byincorporating a monomer such as a polyhydric alcohol or a poly (at leasttri-) hydric carboxylic acid is disclosed. The above process provided away to improve the molding and forming properties of the aliphaticpolyester resin by introducing the monomers into the reactor to reducethe reaction time and to diffuse the molecules within the product.However, the application of this type of polyester resin was not easydue to the decrease of physical properties such as tensile strengthresulted from the drastic increase in low molecular weight polyesters.Besides, the fact that the polyester resin easily becomes a gel typemakes it difficult to control the reaction for preparing the polyesterresin. There is still another process for increasing the molecularweight of the aliphatic polyester resin. Unexamined Korean PatentPublication No. 95-25072, which discloses the high molecular weightaliphatic polyester resin produced by an isocyanate as a couplingmaterial reacting to an aliphatic polyester resin having a numberaverage molecular weight of 15,000 to 20,000 which is produced bydehydration or de-glycol reaction of the mixture of main materials of(1) an aliphatic(including cyclic type), and (2) an aliphatic (includingcyclic type) dicarboxylic acid(or an anhydride thereof) with or without(3) a little of monomer of polyhydric alcohol or polyhydric carboxylicacid (or acid anhydride thereof). The aliphatic polyester resin obtainedin this way had a number average molecular weight of 20,000 to 70,000.However, the above-mentioned process has a few drawbacks that itrequires more reaction time thus resulting in poor productivity, and theisocyanate, a coupling material to increase the molecular weight ofpolyester resin, is known to be a carcinogen so necessitating anextremely careful handling of the ingredient.

On top of that there has not been found a good resolution how to dealwith the waste disposal of syringes nor the syringes ever manufacturedby using biodegradable polyester resins.

SUMMARY OF THE INVENTION

The conventional disposable syringes used in medical fields have been acause of environmental contamination while its biodegradable versionshave been experiencing the limited applications due to their poorphysical properties. The object of the invention is therefore to providea disposable syringe which can not only be degraded in nature withoutcausing an environmental contamination but be applied in a broader fieldof medical industry by having superior physical.

BRIEF DESCRIPTION OF DRAWINGS

FIG. 1 shows a biodegradable disposable syringe manufactured accordingto the method of the present invention.

DESCRIPTION OF THE INVENTION

The present invention relates to a disposable syringe manufactured bymeans of injection molding using biodegradable polyester resin having9,000-90,000 of number average molecular weight, 30,000-600,000 ofweight average molecular weight, 40-150° C. of melting point, 0.1-50g/10min of melt index (190° C., 2160g).

The resin composition used in the present invention comprises anaromatic dicarboxylic acid(or an acid anhydride thereof) such asdimethyl terephthalate and terephthalic acid; an aliphatic (includingcyclic type) dicarboxylic acid(or an acid anhydride thereof), one ormore selected from the group consisting of succinic acid and adipicacid; and an aliphatic (including cyclic type) glycol, one or moreselected from the group consisting of 1,4-butanediol and ethyleneglycol, by means of esterification and polycondensation reactions asdisclosed in Unexamined Korean Patent Publication Nos 98-33837,98-33834,99-56991 and 99-58816.

The polyester resin in the present invention is an aliphatic polyesterresin which has superior physical properties sufficient to resolve thelimitations used to be present in the conventional biodegradable typesof resins by improved biodegradability ascribed to its peculiarmolecular structure.

The specific physical properties of the biodegradable polyester resin inthe present invention can be represented as shown in the following Table1.

TABLE 1 Injection Tensile Strength Elongation Biodegradability MP(° C.)(° C.) (kg/cm²) (%) (%) 40-70 130-140 330 700 98 90 140-150 350 700 96100 150-160 400 600 94 110-150 160-170 400 300 90

According to the present invention, the appropriate melting point of theresin ranges from 40 to 150° C., preferably from 100 to 150° C. If themelting point is below the above range the forming becomes hard toadjust properly due to low crystallinity. Products manufactured by meansof injection molding as in the syringe of the present invention are usedin general for producing relatively hard and durable parts, and thosepolyester resins with higher melting point will be more suitable forinjection molding. If the temperature of injection molding is too low,the resulting syringe products will become too soft to retain itsphysical properties. The melting point of conventional polypropyleneplastic materials falls between 180 and 220° C. and thus the propertiesof those materials are totally different from the one in the presentinvention.

Injection molding using the biodegradable resins of the presentinvention may be performed under general temperature conditions,however, the preferred temperature ranges from 120 to 190° C. If themolding is performed at a temperature lower than 120° C. it is hard toproduce a desirable product because the resin kept within the screw willnot be completely melted, while physical properties become poor due toheat decomposition if it is performed at a temperature higher than 190°C. The conventional PP resin for syringes has different injectionmolding temperature range, 230-275° C. However, if the resins in thepresent invention are molded under temperatures use for conventionalresins, the resins will be inappropriate for molding because they willdecomposed by heat and their physical properties will become extremelypoor. Further, if the resins in the present invention are kept to staywithin the screw of injection for more than 10 min the molding cannot bewell proceeded or the molded product would not be able to carry theproper properties of syringe if they are molded due to heatdecomposition.

For the production of highly durable syringes, the resin may be combinedwith a strength fortifying additive selected from the group consistingof talc, calcium carbonate, magnesium stearate, calcium sulfate,starches, sugar powder, particular anhydrous silicate and calciumphosphate, and preferably by adding 1-60 wt. % of talc or calciumcarbonate based on the 100 wt. % of resin, which then enables to improvethe strength of the resins in the present invention comparable to theconventional resins such as polypropylene, polystyrene or ABS resin.Calcium carbonate is inferior to talc in fortifying strength, however,it can serve as a fertilizer and prevent the soils from acidifying whenit becomes biodegraded and left on the surface of soils after burial. Inaddition, the combustion rate of calcium carbonate added resin wasbetter than those of resin alone or talc-added resin in the presentinvention.

The syringes produced in accordance with the present invention can beproduced in various forms disposable syringe, pre-filled type syringe,general syringe and the like.

For example, FIG. 1 shows a biodegradable disposable syringe of thepresent invention having a needle cap 1, a barrel 2 and a plunger 3manufactured by using a polyester resin composition of the presentinvention under a specific injection molding condition with theexception of the needle.

The following examples are intended to be illustrative of the presentinvention and should not be construed as limiting the scope of thisinvention defined by the appended claims.

PREPARATION EXAMPLE 1

To a 500 mL Erlenmeyer's flask filled with nitrogen gas 118 g ofsuccinic acid, 121.7 g of 1,4-butanediol and 0.1 g of tetrabutyltitanateas a catalyst, were added while slowly increasing the temperature untilit reached 200° C. When the temperature reached 200° C., the reactionmixture was allowed to react for 2 hrs and then theoretical mass ofwater was effused. Then 0.1 g of antimony acetate, 0.2 g of dibutyltinoxide, 0.07 g of tetrabutyltitanate as catalysts, and 0.2 g of trimethylphosphate as a stabilizer were added. The temperature was raised and apolycondensation reaction was performed under 0.3 torr at 245° C. for1.55 min. The sample of biodegradable resin taken at this point had amelt index of 15 (190° C., 2160 g), number average molecular weight of31,000, weight average molecular weight of 190,000 and melting point of117° C. as measured by DSC method.

PREPARATION EXAMPLE 2

To a 500 mL Erlenmeyer's flask filled with nitrogen gas, 5.9 g ofsuccinic acid, 6.3 g of 1,4-butanediol and 0.1 g of tetrabutyltitanateas a catalyst were added to carry esterification by effusing water whileslowly increasing the temperature. When the temperature reached 200° C.,theoretical mass of water was effused completely to give 8.6 g ofaliphatic low molecular weight polymer with its molecular weight around10,000. Then, 76.1 g of terephthalic acid, 135.2 g of 1,4-butanediol,and 0.2 g of tetrabutyltitanate a catalyst were added to the reactionmixture to carry esterification by effusing methanol while slowlyincreasing the temperature. After methanol was effused completely whilekeeping the temperature at 205° C., 29.5 g of succinic acid and 43.8 gof adipic acid were added to carry further esterification. After waterwas effused while keeping the temperature at 180° C., 0.1 g of antimonytrioxide, 0.3 g of dibutyltin oxide, 0.07 g of tetrabutyltitanate ascatalysts, and 0.2 g of trimethyl phosphate as a stabilizer were added.The temperature was raised until it reached 245° C. and apolycondensation reaction was performed under 0.3 torr at 245° C. for200 min. The sample of biodegradable resin taken at this point had amelt index of 2 (1.90° C., 2160 g), number average molecular weight of61,000, weight average molecular weight of 290,000 and melting point of117° C. as measured by DSC method.

EXAMPLE 1˜2

Disposable syringes were manufactured by using polyester resins having117° C. of melting point produced in the above Preparation Examples 1and 2 under 1.30-1.40° C. by means of injection molding. The testresults of syringes showed that 400 kg/cm² and 410 kg/cm² for tensilestrength, 300% and 320% for elongation, and 90% and 92% forbiodegradability rate after 45 days, respectively.

The biodegradability was measured by Organic WasteSystems[O.W.S.n.v.](Dok Noord 4, B-9000 Gent, Belgium), and tensilestrength and elongation were measured by UTM.

What is claimed is:
 1. A biodegradable disposable syringe manufacturedby means of injection molding using biodegradable polyester resincomposition having number average molecular weight of 9,000-90,000,weight average molecular weight of 30,000-600,000, melting point of40-1.50° C., and melt index (190° C., 2160 g) of 0.1-50 g/10 min.
 2. Thebiodegradable disposable syringe according to claim 1, wherein saidpolyester resin composition is an aliphatic polyester resincomprising: 1) an aromatic dicarboxylic acid which contains an aromaticgroup; 2) succinic acid or adipic acid; 3) 1,4-butanediol or ethyleneglycol; and manufactured by esterification and polycondensation.
 3. Thebiodegradable disposable syringe in accordance to claim 1, wherein talcor calcium carbonate is added as a strength fortifier in the ratio of1-60% by weight to said polyester resin composition.
 4. Thebiodegradable disposable syringe in accordance to claim 1, wherein saidinjection molding is performed at 150-220° C.
 5. The biodegradabledisposable syringe in accordance to claim 1, wherein melting temperatureof said polyester resin is 100-150° C.
 6. The biodegradable disposablesyringe in accordance to claim 1, wherein the types of said syringesinclude a general disposable syringe, a pre-filled type syringe and ageneral syringe.
 7. The biodegradable disposable syringe of claim 2,wherein the aromatic dicarboxylic acid or the acid anhydride thereof isdimethyl phthalate or terephthalic acid.
 8. The biodegradable disposablesyringe according to claim 1, wherein said polyester resin compositionis an aliphatic polyester resin comprising: 1) an aromatic dicarboxylicacid or an acid anhydride thereof which contains an aromatic group; 2)an aliphatic dicarboxylic acid or an acid anhydride thereof; 3) analiphatic glycol; and manufactured by esterification andpolycondensation.
 9. The biodegradable disposable syringe of claim 8,wherein the aromatic dicarboxylic acid or the acid anhydride thereof isdimethyl phthalate or terephthalic acid.
 10. The biodegradabledisposable syringe of claim 8, including a cyclic-type aliphaticdicarboxylic acid.
 11. The biodegradable disposable syringe of claim 8,including a cyclic-type aliphatic glycol.
 12. A disposable syringe bythe polycondensation of dicarboxylic acid and a glycol, the syringecomprising: a biodegradable polyester resin composition prepared bypolycondensation after esterification of (i) an aromatic dicarboxylicacid or an anhydride thereof selected from the group consisting ofdimethyl terephthalate and terephthalic acid, and (ii) succinic acid ora mixture of succinic acid and adipic acid with (iii) succinic acid or amixture of succinic acid and adipic acid with an aliphatic glycolselected from the group consisting of 1,4-butanediol and ethyleneglycol, wherein said polyester resin has a number average molecularweight of 9,000-90,000, a weight average molecular weight of30,000-600,000, a melting point of 100-150° C., and a melt index (190°C., 2160 g) of 0.1-50 g/10 min, and wherein said syringe is produced byinjection molding at above 150-190° C.